NeoBiotech Global Corporation
FDA inspection history in Auburn, Washington, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Auburn, Washington.
Cited most
Across all NeoBiotech Global observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.125(a)Labeling issuance1
- 21 CFR 211.165(a)Testing and release for distribution1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.198(a)Complaint files1
The complete NeoBiotech Global file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Auburn, Washington
One Form 483 · 2019 · 8 observations
Latest: Form 483, May 13, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-13 | 483 Form 483 | Auburn, Washington | 8 | $99 |
Investigators on these documents
FEI number 3011869023 · most recent document May 13, 2019
About NeoBiotech Global Corporation
How many FDA Form 483s has NeoBiotech Global Corporation received?
FDA Intel has 1 Form 483 on file for NeoBiotech Global Corporation; the most recent is dated May 13, 2019.
When was NeoBiotech Global Corporation last inspected by FDA?
The most recent FDA inspection document on file for NeoBiotech Global Corporation is a Form 483 dated May 13, 2019, for the site in Auburn, Washington.
What did FDA cite at NeoBiotech Global Corporation?
The regulations cited most in the observations on file for NeoBiotech Global Corporation are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.125(a) (Labeling issuance), 1 time; 21 CFR 211.165(a) (Testing and release for distribution), 1 time.